Key points are not available for this paper at this time.
Bromodomain inhibition comprises a promising therapeutic strategy for KRAS-mutant NSCLC with wild-type LKB1, via inhibition of MYC function. Clinical studies of BET bromodomain inhibitors in aggressive NSCLC will be actively pursued. Clin Cancer Res; 19(22); 6183-92. ©2013 AACR.
Building similarity graph...
Analyzing shared references across papers
Loading...
Takeshi Shimamura
Zhao Chen
Margaret Soucheray
Clinical Cancer Research
Harvard University
Brigham and Women's Hospital
Dana-Farber Cancer Institute
Building similarity graph...
Analyzing shared references across papers
Loading...
Shimamura et al. (Tue,) studied this question.
www.synapsesocial.com/papers/69e0818ad4cf97f1f4c11dc3 — DOI: https://doi.org/10.1158/1078-0432.ccr-12-3904